Organic synthesis of 1,2-dipalmitoyl-rac-glycero-3-phosphatidylethanolamine and its effect on the induction of apoptosis in normal human lung fibroblasts

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemistry and Physics of Lipids Pub Date : 2023-11-01 DOI:10.1016/j.chemphyslip.2023.105349
Beatriz Tlatelpa-Romero , David Atahualpa Contreras-Cruz , Gabriel Guerrero-Luna , María Guadalupe Hernández-Linares , Sinuhé Ruiz-Salgado , Criselda Mendoza-Milla , Yair Romero , René de-la-Rosa Paredes , Luis F. Oyarzábal , Diego Alejandro Mendoza-Sámano , Jiovani Alfredo Galván-León , Luis G. Vázquez-de-Lara
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Abstract

Background /objective

The phospholipid 1,2-dipalmitoyl-rac-glycero-3-phosphatidylethanolamine (PE) comprises two fatty acid chains: glycerol, phosphate, and ethanolamine. PE participates in critical cellular processes such as apoptosis and autophagy, which places it as a target for designing new therapeutic alternatives in diseases such as pulmonary fibrosis. Therefore, this study aimed obtain PE through a six-step organic synthesis pathway and determine its biological effect on apoptosis induction in normal human lung fibroblasts (NHLF).

Methodology

The first step of the organic synthesis route began with protected glycerol that was benzylated at sn-3; later, it was deprotected to react with palmitic acid at sn-1, sn-2. To remove the benzyl group, hydrogenation was performed with palladium on carbon (Pd/C); subsequently, the molecule was phosphorylated in sn-3 with phosphorus oxychloride and triethylamine, and the intermediate was hydrolyzed in an acid medium to obtain the final compound. After PE synthesis, apoptosis assessment was performed: apoptosis was induced using exposure to annexin V-FITC/propidium iodide-ECD (PI) and quantified using flow cytometry. The experiments were performed in three NHLF cell lines with different concentrations of PE 10, 100 and 1000 µg/mL for 24 and 48 h.

Results

The PE obtained by organic synthesis presented a melting point of 190–192 °C, a purity of 95%, and a global yield of 8%. The evaluation of apoptosis with flow cytometry showed that at 24 h, exposure to PE 10, 100, and 1000 µg/mL induces early apoptosis in 19.42%− 25.54%, while late apoptosis was only significant P < 0.05 in cells challenged with 100 µg/mL PE. At 48 h, NHLF exposed to PE 10, 100, and 1000 µg/mL showed decreasing early apoptosis: 28.69–32.16%, 12.59–18.84%, and 10.91–12.61%, respectively. The rest of the NHLF exposed to PE showed late apoptosis: 12.03–16–42%, 11.04–15.94%, and 49.23–51.28%. Statistical analysis showed a significance P < 0.05 compared to the control.

Conclusion

The organic synthesis route of PE allows obtaining rac-1,2-O-Dipalmitoyl-glycero-3-phosphoethanolamine (1), which showed an apoptotic effect on NHLF.

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1,2-二棕榈酰-rac-甘油-3-磷脂酰乙醇胺的有机合成及其对正常人肺成纤维细胞凋亡诱导作用。
背景/目的:磷脂1,2-二棕榈酰-rac-甘油-3-磷脂酰乙醇胺(PE)由甘油、磷酸盐和乙醇胺两条脂肪酸链组成。PE参与细胞凋亡和自噬等关键细胞过程,这使其成为设计肺纤维化等疾病新治疗方案的靶点。因此,本研究旨在通过六步有机合成途径获得PE,并确定其对正常人肺成纤维细胞(NHLF)凋亡诱导的生物学作用;随后,它被脱保护以在sn-1、sn-2处与棕榈酸反应。为了除去苄基,用碳载钯(Pd/C)进行氢化;随后,该分子在sn-3中用三氯氧磷和三乙胺磷酸化,中间体在酸性介质中水解得到最终的化合物。PE合成后,进行细胞凋亡评估:使用膜联蛋白V-FITC/碘化丙啶ECD(PI)诱导细胞凋亡,并使用流式细胞术定量。实验在三种不同浓度PE 10、100和1000µg/mL的NHLF细胞系中进行,持续24小时和48小时。结果:通过有机合成获得的PE熔点为190-192°C,纯度为95%,总收率为8%。流式细胞术对细胞凋亡的评估显示,在24小时内,暴露于PE 10、100和1000µg/mL可诱导19.42%-25.54%的早期细胞凋亡,而晚期细胞凋亡仅为显著P。结论:PE的有机合成途径可获得rac-1,2-O-二棕榈酰甘油-3-磷酸乙醇胺(1),其对NHLF表现出凋亡作用。
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来源期刊
Chemistry and Physics of Lipids
Chemistry and Physics of Lipids 生物-生化与分子生物学
CiteScore
7.60
自引率
2.90%
发文量
50
审稿时长
40 days
期刊介绍: Chemistry and Physics of Lipids publishes research papers and review articles on chemical and physical aspects of lipids with primary emphasis on the relationship of these properties to biological functions and to biomedical applications. Accordingly, the journal covers: advances in synthetic and analytical lipid methodology; mass-spectrometry of lipids; chemical and physical characterisation of isolated structures; thermodynamics, phase behaviour, topology and dynamics of lipid assemblies; physicochemical studies into lipid-lipid and lipid-protein interactions in lipoproteins and in natural and model membranes; movement of lipids within, across and between membranes; intracellular lipid transfer; structure-function relationships and the nature of lipid-derived second messengers; chemical, physical and functional alterations of lipids induced by free radicals; enzymatic and non-enzymatic mechanisms of lipid peroxidation in cells, tissues, biofluids; oxidative lipidomics; and the role of lipids in the regulation of membrane-dependent biological processes.
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